Canonical Allele Identifier: CA349042203

Gene: GALNT3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165765058T>G , CM000664.2:g.165765058T>G	GRCh38
NC_000002.11:g.166621568T>G , CM000664.1:g.166621568T>G	GRCh37
NC_000002.10:g.166329814T>G	NCBI36
NG_012069.1:g.34236A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392701.8:c.516-2A>C MANE Select	ENSP00000376465.3:n.516-2A>C
ENST00000392701.7:c.516-2A>C	ENSP00000376465.3:n.516-2A>C
ENST00000412248.5:c.516-2A>C	ENSP00000412643.1:n.516-2A>C
NM_004482.3:c.516-2A>C	NP_004473.2:n.516-2A>C
XM_005246449.1:c.516-2A>C	XP_005246506.1:n.516-2A>C
XM_006712402.2:c.516-2A>C	XP_006712465.1:n.516-2A>C
XM_011510929.1:c.516-2A>C	XP_011509231.1:n.516-2A>C
XM_017003770.1:c.516-2A>C	XP_016859259.1:n.516-2A>C
XR_002959253.1:n.857-2A>C
NM_004482.4:c.516-2A>C MANE Select	NP_004473.2:n.516-2A>C